Canonical Allele Identifier: CA352183
Gene: USP9X HGNC NCBI

Linked Data

ClinVar Variation Id: 223096
ClinVar RCV Id: RCV000208730
dbSNP Id: rs869025590
MyVariant Identifiers: chrX:g.41029255_41029256insA (hg19) chrX:g.41170002_41170003insA (hg38)
PubMed: PMID:26833328
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41170002_41170003insA , CM000685.2:g.41170002_41170003insA GRCh38
NC_000023.10:g.41029255_41029256insA , CM000685.1:g.41029255_41029256insA GRCh37
NC_000023.9:g.40914199_40914200insA NCBI36
NG_012547.1:g.89368_89369insA

Transcript Alleles

HGVS Amino-acid change
ENST00000703986.1:c.2659_2660insA ENSP00000515603.1:p.Arg887GlnfsTer3
ENST00000703987.1:c.2659_2660insA ENSP00000515604.1:p.Arg887GlnfsTer3
ENST00000704649.1:c.2644_2645insA ENSP00000515974.1:p.Arg882GlnfsTer3
ENST00000704650.1:c.2644_2645insA ENSP00000515975.1:p.Arg882GlnfsTer3
ENST00000704651.1:c.2491_2492insA ENSP00000515976.1:p.Arg831GlnfsTer3
ENST00000704652.1:c.1874_1875insA
ENST00000704653.1:c.1124_1125insA ENSP00000515978.1:n.1124_1125insA
ENST00000324545.9:c.2644_2645insA ENSP00000316357.6:p.Arg882GlnfsTer3
ENST00000378308.7:c.2644_2645insA MANE Select ENSP00000367558.2:p.Arg882GlnfsTer3
ENST00000324545.8:c.2644_2645insA ENSP00000316357.6:p.Arg882GlnfsTer3
ENST00000378308.6:c.2644_2645insA ENSP00000367558.2:p.Arg882GlnfsTer3
NM_001039590.2:c.2644_2645insA NP_001034679.2:p.Arg882GlnfsTer3
NM_001039591.2:c.2644_2645insA NP_001034680.2:p.Arg882GlnfsTer3
XM_005272675.3:c.2659_2660insA XP_005272732.1:p.Arg887GlnfsTer3
XM_005272676.3:c.2659_2660insA XP_005272733.1:p.Arg887GlnfsTer3
XM_005272675.4:c.2659_2660insA XP_005272732.1:p.Arg887GlnfsTer3
XM_005272676.4:c.2659_2660insA XP_005272733.1:p.Arg887GlnfsTer3
NM_001039591.3:c.2644_2645insA MANE Select NP_001034680.2:p.Arg882GlnfsTer3
NM_001039590.3:c.2644_2645insA NP_001034679.2:p.Arg882GlnfsTer3
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